Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due to Subpotent Drug: low out of specification (OOS) test...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lupin Pharmaceuticals Inc. directly.
Affected Products
Cefixime for Oral Suspension USP, 100mg/5mL, Rx Only, Manufactured for: Lupin Pharmaceutical, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Mandideep 462 046 INDIA, NDC 68180-405-01
Quantity: 4,518 bottles
Why Was This Recalled?
Subpotent Drug: low out of specification (OOS) test result observed in long term stability study.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals Inc. has 119 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report